Mycone Dental Supply Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Seity 37% Phosphoric Acid Etchant Gel Ref K112597
Regimes: 510(k) Registry: 510(k)Diamond D High Impact Denture Acrylic Ref K032773
Regimes: 510(k) Registry: 510(k)Mizzy Express Ref K093380
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mycone Dental Supply Co., Inc. have in the registry?
The registry currently lists 3 devices for Mycone Dental Supply Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mycone Dental Supply Co., Inc.'s devices?
Among its 3 most recently registered devices, Mycone Dental Supply Co., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Mycone Dental Supply Co., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mycone Dental Supply Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mycone Dental Supply Co., Inc. in the registry?
The most recently registered devices listed for Mycone Dental Supply Co., Inc. include SEITY 37% PHOSPHORIC ACID ETCHANT GEL, DIAMOND D HIGH IMPACT DENTURE ACRYLIC and MIZZY EXPRESS.